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Benzyl-O-(2,3,4-tri-O-benzoyl-6-desoxy-β-D-galactopyranosyl)-(1->3)-2-acetamido-4,6-di-O-acetyl-2-desoxy-α-D-galactopyranosid

Base Information
  • Chemical Name:Benzyl-O-(2,3,4-tri-O-benzoyl-6-desoxy-β-D-galactopyranosyl)-(1->3)-2-acetamido-4,6-di-O-acetyl-2-desoxy-α-D-galactopyranosid
  • CAS No.:141020-12-4
  • Molecular Formula:C46H47NO15
  • Molecular Weight:853.877
  • Hs Code.:
Benzyl-O-(2,3,4-tri-O-benzoyl-6-desoxy-β-D-galactopyranosyl)-(1->3)-2-acetamido-4,6-di-O-acetyl-2-desoxy-α-D-galactopyranosid

Synonyms:Benzyl-O-(2,3,4-tri-O-benzoyl-6-desoxy-β-D-galactopyranosyl)-(1->3)-2-acetamido-4,6-di-O-acetyl-2-desoxy-α-D-galactopyranosid

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Chemical Property of Benzyl-O-(2,3,4-tri-O-benzoyl-6-desoxy-β-D-galactopyranosyl)-(1->3)-2-acetamido-4,6-di-O-acetyl-2-desoxy-α-D-galactopyranosid
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Technology Process of Benzyl-O-(2,3,4-tri-O-benzoyl-6-desoxy-β-D-galactopyranosyl)-(1->3)-2-acetamido-4,6-di-O-acetyl-2-desoxy-α-D-galactopyranosid

There total 13 articles about Benzyl-O-(2,3,4-tri-O-benzoyl-6-desoxy-β-D-galactopyranosyl)-(1->3)-2-acetamido-4,6-di-O-acetyl-2-desoxy-α-D-galactopyranosid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 6 steps
1: 92 percent / 70 percent HClO4 / 2 h
2: 78 percent / piperidine / tetrahydrofuran / 18 h / Ambient temperature
3: 95 percent / 1,5-diazabocyclo<5.4.0>undec-5-ene / CH2Cl2 / 3 h / Ambient temperature
4: 1.) molecular sieves 4 Angstroem, 2.) trimethylsilyl triflate / 1.) dichloromethane, 1 h, 2.) r.t., 5 h
5: 60 percent aq. acetic acid / 2 h / 40 °C
6: pyridine / 48 h
With piperidine; pyridine; perchloric acid; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; acetic acid; 1,5-Diazabicyclo[5.4.0]undec-5-ene; In tetrahydrofuran; dichloromethane;
Guidance literature:
Multi-step reaction with 6 steps
1: 78 percent / molecular sieves 4 Angstroem, SnCl4 / CH2Cl2 / 2 h / -20 °C
2: 0.1 N methanolic NaOMe / methanol / 3 h
3: pyridine / 10 h
4: 1.) molecular sieves 4 Angstroem, 2.) dimethyl(methylthio)sulfonium triflate / 1.) dichloromethane, 1 h, 2.) r.t., 3 h
5: 60 percent aq. acetic acid / 2 h / 40 °C
6: pyridine / 48 h
With pyridine; 4 A molecular sieve; sodium methylate; tin(IV) chloride; acetic acid; dimethyl-(methylthio)-sulphonium trifluoromethanesulphonate; In methanol; dichloromethane;
Guidance literature:
Multi-step reaction with 5 steps
1: 0.1 N methanolic NaOMe / methanol / 3 h
2: pyridine / 10 h
3: 1.) molecular sieves 4 Angstroem, 2.) dimethyl(methylthio)sulfonium triflate / 1.) dichloromethane, 1 h, 2.) r.t., 3 h
4: 60 percent aq. acetic acid / 2 h / 40 °C
5: pyridine / 48 h
With pyridine; 4 A molecular sieve; sodium methylate; acetic acid; dimethyl-(methylthio)-sulphonium trifluoromethanesulphonate; In methanol;
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